Actively Recruiting
Understanding Painful Inflammation in Patellofemoral Joint Osteoarthritis Using [18F] FDG PET/MRI Imaging
Led by University of California, San Francisco · Updated on 2026-06-04
50
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating painful inflammation in the patellofemoral joint affected by osteoarthritis (PFJ OA) using a combined imaging method called [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET) and magnetic resonance imaging (MRI). This method aims to detect pain-related inflammation by measuring glucose usage in tissues and detailed anatomy of the knee. The study focuses on distinguishing normal metabolic activity caused by weight-bearing from abnormal inflammation linked to pain in patients with PFJ OA compared to people without symptoms. The study involves two main parts. First, participants will undergo PET/MRI scans of the unloaded knee to measure FDG uptake in painful areas and compare these between PFJ OA patients and matched healthy controls. Then, participants will have a second PET/MRI scan while the knee is loaded with 25% of body weight using a custom device to assess changes in inflammation under stress. Biomechanical measurements during physical tests like single-leg squats will also be collected to analyze their relationship with imaging results. Participants will be adults able to perform 25 single-leg squats and without recent traumatic knee injuries or contraindications to MRI or PET. They will complete imaging sessions in both unloaded and loaded knee states, followed by physical performance tests. Researchers will measure maximum standardized uptake values (SUVmax) of FDG in knee tissues before and after loading, and evaluate pain scores during squats. This approach aims to improve understanding of inflammation and pain in PFJ OA, supporting development of better diagnostic and treatment methods. The study is expected to continue until February 2028.
CONDITIONS
Brief Title
FDG PET/MRI Imaging of Patellofemoral Joint Osteoarthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult with the capacity to give informed consent
- Ability to perform 25 single-leg squats
- No traumatic knee injuries or surgeries since last visit for the parent study
- No investigational drugs since last visit for the parent study
- No contraindications to MRI or PET tracer since last visit for the parent study
- Not taking steroid injections
- Not pregnant
- For healthy volunteers: minimal pain (VAS=0-1) during 25 single-leg squats on one or both legs
You will not qualify if you...
- Inability to consent for themselves
- Inability to perform 25 single-leg squats with the study leg
- New traumatic knee injuries or surgeries since last visit for the parent study
- Taking investigational drugs since last visit for the parent study
- New contraindications to MRI or PET tracer since last visit for the parent study
- Taking steroid injections
- Pregnant
- Diabetic
- For healthy volunteers: VAS of 2 or greater during 25 single-leg squats on both legs
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo FDG PET/MRI imaging of the knee in unloaded and loaded conditions to identify painful inflammation and hypermetabolic activity related to patellofemoral joint osteoarthritis.
1 imaging visit including unloaded and loaded knee scans
Duration - Same day as imaging
Participants complete a battery of physical performance tests for biomechanical measurements following imaging.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
UCSF Radiology China Basin
San Francisco, California, United States, 94107
Actively Recruiting
Research Team
E
Eric Hammond
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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